Perfluoroalkanoyl aminonitriles

ABSTRACT

There are provided perfluoroalkanoyl aminonitrile intermediates and their use in a facile and efficient synthesis of 2-perfluoroalkyl-3-oxazolin-5-one. Said oxazolinone is a key intermediate in the preparation of insecticidal, acaricidal and nematocidal pyrrole compounds.

This is a divisional of application Ser. No. 08/175,845 filed on Dec.30, 1993 now U.S. Pat. No. 5,426,225.

BACKGROUND OF THE INVENTION

Arylpyrrole carbonitrile compounds and derivatives thereof are highlyeffective insecticidal, acaricidal and nematocidal agents. In particular2-aryl-5-trifluoromethylpyrrole-3-carbonitrile compounds and theirderivatives have been found to have a broad spectrum of activity at verylow rates of application with effectiveness against resistant species.U.S. Pat. No. 5,030,735 describes methods to prepare said pyrrolecompounds on a manufacturing scale and includes the 1,3-dipolarcycloaddition of the appropriate 3-oxazolin-5-one with2-chloroacrylonitrile. Heretofore the 3-oxazolin-5-one key intermediatehas been prepared through the appropriate phenylglycine compound in a 4step synthetic route from the preceding aminonitrile.

It is an object of this invention to provide perfluoroalkanoylaminonitrile compounds useful in preparing2-perfluoroalkyl-3-oxazoline-5-one.

It is a further object of this invention to provide a convenient sourceof a key intermediate in the manufacture of insecticidal, acaricidal andnematocidal arylpyrrole compounds.

SUMMARY OF THE INVENTION

There is provided a perfluoroalkanoyl aminonitrile intermediate offormula I ##STR1## wherein n is an integer of 1, 2, 3, 4, 5, 6, 7 or 8;

R is ##STR2## L is hydrogen or halogen; M and Q are each independentlyhydrogen, halogen, CN, NO₂, C₁ -C₄ alkyl, C₁ -C₄ haloalkyl, C₁-C4alkoxy, C₁ -C₄ haloalkoxy, C₁ -C₄ alkylthio, C₁ -C₄ alkylsulfinyl orwhen M and Q are on adjacent positions they may be taken together withthe carbon atoms to which they are attached to form a ring in which MQrepresents the structure

    --OCH.sub.2 O--, --OCF.sub.2 O-- or --CH═CH--CH═CH--

with the proviso that at least one of L, M and Q must be other thanhydrogen;

R₁, R₂ and R₃ are each independently hydrogen, halogen, NO₂, CHO or R₂and R₃ may be taken together with the atoms to which they are attachedto form a ring in which R₂ R₃ is represented by the structure ##STR3##R₄, R₅, R₆ and R₇ are each independently hydrogen, halogen, CN or NO₂ ;and

W is O or S.

The formula I perfluoroalkanoyl aminonitrile is useful in thepreparation of 2-perfluoroalkyl-3-oxazolin-5-one which is a keyintermediate in the manufacture of insecticidal, acaricidal andnematocidal pyrrole compounds. The preparation of2-perfluoroalkyl-3-oxazolin-5-one is described in co-pending patentapplication Ser. No. 08/175,822, (Attorney Docket No. 32,356) filedconcurrently herewith.

DETAILED DESCRIPTION OF THE INVENTION

Arylpyrrole compounds, particularly2-aryl-5-trifluoromethylpyrrole-3-carbonitrile compounds are a new classof highly effective insecticidal, acaricidal and nematocidal agents. Akey intermediate in their preparation is the2-perfluoroalkyl-3-oxazolin-5-one compound of formula II ##STR4##wherein n and R are as described hereinabove for formula I. Methodscurrently known to prepare the formula II oxazolinone involve thepreparation of the appropriate arylglycine V via hydrolysis of theaminonitrile III. The aminonitrile is obtained via the Streckersynthesis from the appropriate aldehyde (W. L. Matier et al, J. Med.Chem.,1973, 16,901). Protection of the amino group in the aminonitrileIII by acetylation to VI followed by acidic hydrolysis of both the cyanoand the protecting groups is required due to the instability of theaminonitrile III under hydrolysis conditions. The thus-obtained glycineV is then trifluoroacetylated to give VII and cyclized to give thedesired oxazolinone II in 4 steps. This procedure is shown in flowdiagram I, wherein R is p-chlorophenyl and n is 1. ##STR5##

It has now been found that direct perfluoroacylation of the Streckerproduct III gives the perfluoroalkanoyl aminonitrile I which may bereadily converted to the desired 2-perfluoroalkyl-3-oxazolin-5-one II.The reaction is shown in flow diagram II wherein m is 1 or 2, X is Cl,OR₁ or O and R₁ is hydrogen or C₁ -C₆ alkyl with the proviso that when Xis O, then m must be 2 and when X is Cl or OR₁, then m must be 1.##STR6##

Surprisingly, the perfluoroalkanoyl aminonitrile of formula I may becyclized in a single step in good yield under aqueous acid conditions tothe 2-perfluoroalkyl-3-oxazolin-5-one compound of formula II.

Preferred compounds of formula I are those wherein n is 1, 2 or 3 andmore preferred are those wherein n is 1. Also preferred are thosecompounds of formula I wherein R is phenyl optionally substituted withone to three halogen, NO₂, C₁ -C₄ haloalkyl or C₁ -C₄ haloalkoxy groups.

In accordance with the method of invention, an aminonitrile of formulaIII is admixed with approximately an equimolar amount of aperfluoroacylating agent of formula IV in the presence of a solvent,optionally in the presence of a base, to form the perfluoroalkanoylaminonitrile of formula I. The formula I compound is then cyclized inthe presence of an aqueous acid to form the formula II compound,2-perfluoralkyl-3-oxazolin-5 one.

Solvents suitable for use in the method of invention are aromatichydrocarbons, or halogenated aromatic hydrocarbons, preferably aromatichydrocarbons such as toluene, benzene, xylene and the like, morepreferrably, toluene.

Acids suitable for use in the method of invention include sulfuric acid,methanesulfonic acid benzenesulfonic acid, p-toluenesulfonic acid,naphthalenesulfonic acid, fluoroboric acid, boron trifluoride complexesand the like. Boron trifluoride complexes may include BF₃ etherate, BF₃methanol complex, BF₃ ethanol complex, BF₃ dihydrate and the like. Watermay be introduced as a hydrate, i.e. p-toluensulfonic acid monohydrateor as a solute such as 30%-60% aqueous sulfuric acid.

In actual practice, if a perfluoroacyl chloride, such as trifluoroacetylchloride, is used as the formula IV reagent, then an equimolar amount ofa base may be added as an HCl scavenger. Among the bases which may beused are alkali metal carbonates such as sodium carbonate or potassiumcarbonate or alkali metal bicarbonates such as sodium or potassiumbicarbonate or mixtures thereof or tertiary amines.

Tertiary amines suitable for use in the method of invention are any ofthose well known in the art such as trialkylamine, dialkylarylamine,triarylamine, and the like preferably trialkylamine, more preferablytriethylamine.

In order to provide a more clear understanding of the invention, thefollowing examples are set forth below. These examples are merelyillustrative and are not to be understood to limit the scope orunderlying principles of the invention in any way.

The terms ¹ H, ¹³ C and ¹⁹ FNMR designate proton, carbon 13 and fluorine19 nuclear magnetic resonance, respectively.

EXAMPLE 1 Preparation ofN-[(p-Chlorophenyl)cyanomethyl]-2,2,2-trifluoroacetamide ##STR7##

Method A: A stirred slurry of α-cyano-p-chlorobenzylamine (250 g, 1.5mol) in toluene is treated with trifluoroacetic anhydride (315 g, 1.5mol) at 35° C. over a 90 minute period. The mixture is treated withheptane, the resultant precipitate is filtered and the filter-cake iswashed with toluene/heptane to give the title product, 323.7 g, 82%yield, mp 127°-128° C., identified by ¹ H, ¹³ C and ¹⁹ FNMR analyses.

Method B: A solution of α-cyano-p-chlorobenzylamine (83.3 g, 0.5 mol) inmethanol is treated with ethyl trifluoroacetate (85.2 g, 0.6 mol),stirred at room temperature for about 16 hours and concentrated in vacuoto give a residue. The residue is crystallized from toluene/heptane togive the title product as a pale yellow solid, 88.3 g, 67.2% yield, mp127°-128° C.

Method C: A mixture of α-cyano-p-chlorobenzylamine (83.3 g, 0.5 mol) andtriethylamine (50.6 g, 0.5 mol) in toluene is treated dropwise withtrifluoroacetyl chloride (66.2 g, 0.5 mol), stirred at ambienttemperature for about 1 hour and filtered. The filtrate is washed oncewith water and concentrated in vacuo to give a residue. The residue iscrystallized in toluene/hexane to give the title product, 114.2 g, 87%yield, mp 127°-128° C.

EXAMPLE 2 Preparation of N-(Arylcyanomethyl)-2,2,2-trifluoroacetamide##STR8##

Using essentially the same procedure described as Method A in Example 1and substituting the appropriate α-cyanobenzylamine as startingmaterial, the following N-(Arylcyanomethyl) 2,2,2-trifluoroacetamideproducts are obtained. The products are identified by ¹ H, ¹³ C and ¹⁹FNMR analyses.

                  TABLE I                                                         ______________________________________                                         ##STR9##                                                                     L       M       Q         mp °C.                                                                         % Yield                                     ______________________________________                                        H       4-Br    H         128.0-128.5                                                                           76                                          H       4-CF.sub.3                                                                            H         115.0-116.0                                                                           63                                          3-Cl    4-Cl    H         113.0-115.0                                                                           .sup. 35.sup.a                              ______________________________________                                         .sup.a Based on aldehyde used in Strecker synthesis. (Crude Strecker          product used as starting material)                                       

EXAMPLE 3 Preparation of N-(α-Cyanothienyl)-2,2,2-trifluoroacetamide##STR10##

Using essentially the same procedure described as Method A in Example 1and substituting the crude Strecker product,α-cyano-2-thiophenemethylamine, as starting material the title productis obtained in 23% yield^(a), m.p. 73.0°-74.5° C., identified by ¹ H, ¹³C and ¹⁹ FNMR analyses.

EXAMPLE 4 Preparation ofN-[(p-Chlorophenyl)cyanomethyl]-2,2,3,3,4,4,4-heptafluorobutyramide##STR11##

Using essentially the same procedure described as Method A in Example 1and substituting heptafluorobutyric anhydride as the perfluoro-acylatingagent, the title product is obtained as white crystals in 95% yield, mp93.0°-95.0° C., identified by ¹ H, ¹³ C and ¹⁹ FNMR analyses.

EXAMPLE 5 Preparation ofN-[(p-Chlorophenyl)cyanomethyl]-2,2,3,3,3-pentafluoropropionamide##STR12##

Using essentially the same procedure described as Method A in Example 1and substituting pentafluoropropionic anhydride as theperfluoro-acylating agent, the title product is obtained as whitecrystals, 95% yield, mp 118.0°-118.5° C. identified by ¹ H, ¹³ C and ¹⁹FNMR analyses.

EXAMPLE 6 Preparation of4-(p-Chlorophenyl-2-(trifluoromethyl)-3-oxazolin-5-one ##STR13##

Method A: A solution ofN-[(p-chlorophenyl)cyanomethyl]-2,2,2-trifluoroacetamide (0.1 mol) intoluene at 80° C. is treated portion-wise with p-toluene sulfonic acidmonohydrate (p-tsa.H₂ O) (0.11 mol) over an 0.75-1.0 hour period,stirred at 90°-95° C. for 2-3 hours, cooled and filtered. The filtrateis washed twice with water and concentrated in vacuo to give an oilresidue. The oil is dissolved in heptane, filtered and the filtrate isvacuum distilled to give the title product as an oil, 55.6% yield, bp78° C./0.01 mmHg, identified by ¹ H, ¹³ C and ¹⁹ FNMR analyses.

Method B: A solution ofN-[p-(chlorophenyl)cyanomethyl]-2,2,2-trifluoroacetamide (26.3 g, 0.1mol) in toluene and methanesulfonic acid (10.7 g, 0.11 mol) at 80° C. istreated with water (2 mL, 0.11 mol) over a 20 minute period, stirred at90° C. for 8 hours and cooled. The reaction mixture is washed twice withwater. The organic layer is concentrated in vacuo to give an oil whichis vacuum distilled to give the title product as an oil, 13.7 g, bp 80°C./0.01 mm Hg.

EXAMPLE 7 Preparation of4-(2-Thienyl-2-(trifluoromethyl)-3-oxazolin-5-one ##STR14##

Using essentially the same procedure described as Method A in Example 6and substituting N-(α-cyanothienyl)-2,2,2-trifluoroacetamide as startingmaterial, the title product is obtained as a pale brown solid, 50%yield, mp 62.0°-65.0° C., identified by IR and ¹ H, ¹³ C and ¹⁹ FNMRanalyses.

EXAMPLE 8 Preparation of 2-perfluoroalkyl-3-oxazlin-5-one ##STR15##

Using essentially the same procedure described as Method A in Example 6and substituting the appropriate perfluoroalkyanoyl aminonitrile asstarting material, the compounds shown in Table II are obtained.

                  TABLE II                                                        ______________________________________                                         ##STR16##                                                                    L     M        Q      R      mp °C.                                                                           % Yield                                ______________________________________                                        H     4-Br     H      CF.sub.3                                                                             48.0-51.0 64                                     H     4-CF.sub.3                                                                             H      CF.sub.3                                                                             39.0-40.5 55                                     3-Cl  4-Cl     H      CF.sub.3                                                                             103°/0.1 mm.sup.a                                                                54                                     H     4-Cl     H      C.sub.2 F.sub.5                                                                      39.0-42.0 72                                     H     4-Cl     H      n-C.sub.3 H.sub.7                                                                    93.0-95.0 56                                     ______________________________________                                         .sup.a bp° C.                                                     

I claim:
 1. A compound having formula I ##STR17## wherein n is aninteger of 1, 2, 3, 4, 5, 6, 7 or 8;R is ##STR18## L is hydrogen orhalogen; M and Q are on adjacent positions and taken together with thecarbon atoms to which they are attached form a ring in which MQrepresents the structure

    --OCH.sub.2 O--, --OCF.sub.2 O--

with the proviso that at least one of L, M and Q must be other thanhydrogen; R₁, R₂ and R₃ are each independently hydrogen, halogen, NO₂,CHO or R₂ and R₃ may be taken together with the atoms to which they areattached to form a ring in which R₂ R₃ is represented by the structure##STR19## R₄, R₅, R₆ and R₇ are each independently hydrogen, halogen, CNor NO₂ ; and W is O or S.
 2. The compound according to claim 1 wherein nis an integer of 1 to
 2. 3. The compound according to claim 2 whereinRis ##STR20##
 4. The compound according to claim 3 wherein R₁ is in the 3position and is hydrogen.
 5. The compound according to claim 4 whereinR₂ and R₃ are each independently hydrogen or halogen.
 6. The compoundaccording to claim 5 wherein W is S.
 7. The compound according to claim6 N-(α-cyanothienyl)-2,2,2-trifluoroacetamide.